Xanthene

Names
Preferred IUPAC name 9H-Xanthene[1]
Other names Dibenzo[a,e]pyran 10H-9-Oxaanthracene
Identifiers
CAS Number	92-83-1 Y
3D model (JSmol)	Interactive image
Beilstein Reference	133939
ChEBI	CHEBI:10057 Y
ChEMBL	ChEMBL486760 Y
ChemSpider	6840 Y
ECHA InfoCard	100.001.996
EC Number	202-194-4
Gmelin Reference	83576
KEGG	C01464 N
PubChem CID	7107
UNII	A762Z8101Y Y
CompTox Dashboard (EPA)	DTXSID1059070
InChI InChI=1S/C13H10O/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2 N Key: GJCOSYZMQJWQCA-UHFFFAOYSA-N N InChI=1/C13H10O/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2 Key: GJCOSYZMQJWQCA-UHFFFAOYAO
SMILES O1c2ccccc2Cc3ccccc31
Properties
Chemical formula	C13H10O
Molar mass	182.222 g·mol−1
Appearance	Yellow solid
Melting point	101 to 102 °C (214 to 216 °F; 374 to 375 K)[2]
Boiling point	310 to 312 °C (590 to 594 °F; 583 to 585 K)[2]
Hazards[3]
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H317
Precautionary statements	P280
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Xanthene (9H-xanthene, 10H-9-oxaanthracene) is the organic compound with the formula CH₂[C₆H₄]₂O. It is a yellow solid that is soluble in common organic solvents. Xanthene itself is an obscure compound, but many of its derivatives are useful dyes.^[4]

Xanthene dyes

Dyes that contain a xanthene core include bikaverin, fluorescein, eosins, and rhodamines. Xanthene dyes tend to be fluorescent, yellow to pink to bluish red, brilliant dyes. Many xanthene dyes can be prepared by condensation of derivates of phthalic anhydride with derivates of resorcinol or 3-aminophenol.

Further reading

• Neckers, Douglas C.; Valdes-Aguilera Oscar M. (1993). "Photochemistry of the Xanthene Dyes". Advances in Photochemistry. Vol. 18. pp. 315–94. doi:10.1002/9780470133491.ch4. ISBN 9780470133491.

See also

• Xanthone
• Xanthydrol

References